Ank3-Dependent SVZ Niche Assembly Is Required for the Continued Production of New Neurons

被引:106
作者
Paez-Gonzalez, Patricia [1 ,2 ]
Abdi, Khadar [1 ,2 ]
Luciano, Dominic [3 ]
Liu, Yan [1 ]
Soriano-Navarro, Mario [4 ]
Rawlins, Emma [1 ]
Bennett, Vann [1 ,5 ]
Manuel Garcia-Verdugo, Jose [4 ]
Kuo, Chay T. [1 ,2 ,3 ,6 ,7 ]
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Pediat, Brumley Neonatal Perinatal Res Inst, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Neurobiol, Durham, NC 27710 USA
[4] CIBERNED, Unidad Mixta CIPF UVEG, Lab Morfol Celular, Valencia, Spain
[5] Duke Univ, Med Ctr, Howard Hughes Med Inst, Durham, NC 27710 USA
[6] Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Durham, NC 27710 USA
[7] Duke Univ, Inst Brain Sci, Durham, NC 27708 USA
关键词
NEURAL STEM-CELLS; TRANSCRIPTION FACTORS; EPENDYMAL CELLS; VASCULAR NICHE; RADIAL GLIA; EPITHELIAL-CELLS; ADULT; ASTROCYTES; REPAIR; GENE;
D O I
10.1016/j.neuron.2011.05.029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The rodent subventricular/subependymal zone (SVZ/SEZ) houses neural stem cells (NSCs) that generate olfactory bulb interneurons. It is unclear how the SVZ environment sustains neuronal production into adulthood. We discovered that the adapter molecule Ankyrin-3 (Ank3) is specifically upregulated in ventricular progenitors destined to become ependymal cells, but not in NSCs, and is required for SVZ niche assembly through progenitor lateral adhesion. Furthermore, we found that Ank3 expression is controlled by Foxj1, a transcriptional regulator of multicilia formation, and genetic deletion of this pathway led to complete loss of SVZ niche structure. Interestingly, radial glia continued to transition into postnatal NSCs without this niche. However, inducible deletion of Foxj1-Ank3 from mature SVZ ependyma resulted in dramatic depletion of neurogenesis. Targeting a pathway regulating ependymal organization/assembly and showing its requirement for new neuron production, our results have important implications for environmental control of adult neurogenesis and harvesting NSCs for replacement therapy.
引用
收藏
页码:61 / 75
页数:15
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